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Low temperature synthesis of garnet solid state electrolytes: Implications on aluminium incorporation in Li7La3Zr2O12

机译:石榴石固态电解质的低温合成:LI7LA3ZR2O12铝掺入的影响

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摘要

Li ion conducting garnet electrolytes are attracting considerable interest for potential use in all solid state batteries. Nevertheless, their synthesis can be challenging due to the high temperatures required leading to significant Li loss, and consequently the need to add excess Li to counteract this. In this work, we report a low temperature biopolymer sol-gel route to synthesise these garnet materials using Agar (to ensure homogeneous mixing and nucleation through this biotemplating matrix), with the formation of the garnet phase starting at temperatures as low as 600 degrees C, with single phase samples of tetragonal Li7La3Zr2O12, and cubic Li6.4Al0.2La3Zr2O12 prepared at 700 degrees C (similar to 400 degrees C lower than the conventional solid state routes). Significantly, this route also allowed the synthesis of these garnets without the need for Li excess for the first time, due to the low temperature limiting Li loss. Moreover, if Li excess was used in the synthesis of cubic Li6.4Al0.2La3Zr2O12, Al incorporation was not observed at this temperature, and rather tetragonal Li7La3Zr2O12 was obtained. Contrary to previous assumptions, this indicates that the Li is more stable in the structure than Al at low temperature. Thus, Al incorporation only occurs if there is a deficiency of Li in the starting material, or if the sample is heated to elevated temperatures to induce Li volatility, so as to drive the incorporation of Al to charge balance the resultant Li loss.
机译:锂离子导电石榴石电解质吸引了所有固态电池的潜在利益。尽管如此,由于导致显着锂损失所需的高温,它们的合成可能是挑战性的,因此需要增加过量的李来抵消这一点。在这项工作中,我们报告了一种低温生物聚合物溶胶 - 凝胶途径,使用琼脂合成这些石榴石材料(通过该生物预算基质确保均匀混合和成核),在低至600℃的温度下形成石榴石相的形成,用四方Li7la3zR2O12的单相样品,以及在700℃下制备的立方Li6.4Al0.2La3zR2O12(与常规固态路线低400℃)。值得注意的是,由于低温限制锂损失,该途径也允许合成这些装甲而不需要锂过量。另外,如果在立方体Li6.4Al0.2La3Zr2O12的合成中使用Li过量,则在该温度下未观察到Al掺入,并获得四边形Li7La3zR2O12。与先前的假设相反,这表明Li在低温下的结构比Al更稳定。因此,只有在原料中存在Li的缺陷,或者如果将样品加热至升高的温度以诱导锂挥发性,则仅发生Al掺入,从而驱动Al的掺入来对所得锂损失的掺入。

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